Facility

Accora Inc

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3013254491
Establishment type	Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device
Location	6021 University Blvd Ste 530 Ellicott City, MD, US 21043
Registration status	Active · expires 2026
Parent company	Accora Ltd (owner-operator 10052470)
Brand names	Allevia Classic; Allevia Duo; Allevia Prima; Allevia Comfort

Activity by year

Recalls (1)

Devices registered here (1)

Mattress, Flotation Therapy, Non-Powered
Product code IKY (opens in a new tab) · Class I · General Hospital · 21 CFR 880.5150

Recalls & enforcement

Class IIOngoing2021-06-21
The firm has identified a potential for the backrest to become detached from the chair.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Accora Inc (FEI 3013254491) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3013254491-accora-inc/

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